Ireland
--:--IST
Active, not recruiting Not applicable

Effectiveness of a Therapeutic Education Program on Female Sexuality in Women Attending Cardiac Rehabilitation.

NCT07426263 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-02-18
Last updated
2026-05-13

Condition(s) studied

Cardiovascular Diseases

Investigational drug(s) / intervention(s)

Therapeutic Education Program on Female Sexuality (PET-SF)Usual Care

Therapeutic Education Program on Female Sexuality (PET-SF): The PET-SF is a structured, nurse-led, group-based therapeutic education program specifically developed for women undergoing cardiac rehabilitation. Unlike general cardiac education or brief counselling approaches, PET-SF focuses exclusively on female sexuality after cardiovascular disease and integrates clinical safety information with psychosocial and relational dimensions. The program is delivered in four structured sessions over approximately two weeks and is grounded in an educational framework inspired by the EX-PLISSIT model. It combines evidence-based information, normalization of concerns, communication skill development, and practical guidance to support safe resumption of sexual activity within a gender-sensitive approach integrated into routine cardiac rehabilitation.

Usual Care: Participants allocated to the control group will receive usual care as provided within the standard cardiac rehabilitation program. Usual care includes multidisciplinary cardiovascular rehabilitation focusing on physical training, cardiovascular risk factor management, lifestyle modification, and medical follow-up. The control group will not receive the structured PET-SF educational intervention during the main study period. After completion of follow-up assessments, participants in the control group will be offered the opportunity to participate in the PET-SF program.

Study summary

Cardiovascular disease is the leading cause of morbidity and mortality among women and is frequently associated with changes in sexual function, emotional distress, and reduced quality of life. In women, these difficulties are often influenced by gender-specific factors, including differences in clinical presentation, psychosocial roles, caregiving responsibilities, and the historical under-recognition of female sexuality within cardiovascular care. Although international clinical recommendations highlight the importance of addressing sexual health as part of comprehensive cardiac rehabilitation, this aspect remains insufficiently integrated into routine practice, particularly from a female-centered perspective.

This randomized controlled trial aims to evaluate the effectiveness of a Therapeutic Education Program on Female Sexuality (PET-SF), specifically designed and implemented within a hospital-based cardiac rehabilitation unit. The program is delivered as a structured, group-based, nurse-led educational intervention integrated into usual care. The primary outcome is female sexual function, while secondary outcomes include anxiety, depression, quality of life, and medication adherence. The study seeks to determine whether a gender-sensitive therapeutic education approach can improve sexual well-being and related psychosocial outcomes in women attending cardiac rehabilitation.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Women will be eligible to participate if they meet all of the following criteria: * Female sex. * Age 18 years or older. * Referral to a hospital-based Cardiac Rehabilitation Unit following a cardiovascular event. * Clinical stability and medical clearance to participate in the cardiac rehabilitation program. * Ability to understand the study information and provide written informed consent. Exclusion Criteria: Women will be excluded if any of the following criteria apply: * Severe cognitive impairment or language barriers that preclude understanding of the intervention or study procedures. * Recent participation in structured sexual education or sexual counselling programs. * Inability to attend the sessions assigned within the intervention period. * Attendance at fewer than two sessions of the intervention program. * Occurrence of clinical complications or hospital readmission during the study period that prevent continued participation.

Primary outcome measure(s)

  • Female Sexual Function — Change from baseline (T0) to follow-up (T2, 12-13 weeks)
    Instrument: Female Sexual Function Index (FSFI-19). The Female Sexual Function Index is a validated 19-item questionnaire assessing six domains of female sexual function over the previous four weeks: desire, arousal, lubrication, orgasm, satisfaction, and pain. The total score ranges from 2 to 36, with higher scores indicating better sexual function (less dysfunction and less pain). A total score of ≤26-26.55 is commonly used as a threshold suggestive of sexual dysfunction. Clinical improvement will be interpreted as a change from a baseline score \<26 to ≥26 and/or a moderate effect size (≥0.5) in score change over time, in accordance with established interpretation guidelines.

Trial sites (1)

FacilityCityRegionStatus
Virgen Macarena University Hospital. Seville (Spain) Seville Spain
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07426263 on ClinicalTrials.gov ↗ ← All trials in Spain